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Validation Engineer
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Engineering, Engineer, Design
Projektbeschreibung
For a 4 month project with our customer in Basel, we are looking ASAP for a
Validation Engineer
Tasks:
- Independent planning and execution of all required activities for qualification/validation of equipment, special processes and production processes.
- Independent creation of all required qualification/validation documents in cooperation with production, product development, design transfer and quality engineering.
- Serves as technical expert for the Validation process and responsibilities to ensure compliance.
- Ensure that all validation activities are carried out and reported in a timely manner.
- Ability to execute Validation processes and Testing.
Requirements:
- Fluent GERMAN is essential for this position and advanced English.
- 3 Years proven qualification/validation experience in the medical devices production environment.
- Experience in Process Validation, Medical Devices, 21 FDA 820, ISO 13485.
- Engineering background.
- Analytical, innovative and pragmatic thinking.
- Some flexibility in working hours is required.
- Able to follow change management for internal guidelines.
Are you interested in this position? Then we are looking forward to receiving your application.
Validation Engineer
Tasks:
- Independent planning and execution of all required activities for qualification/validation of equipment, special processes and production processes.
- Independent creation of all required qualification/validation documents in cooperation with production, product development, design transfer and quality engineering.
- Serves as technical expert for the Validation process and responsibilities to ensure compliance.
- Ensure that all validation activities are carried out and reported in a timely manner.
- Ability to execute Validation processes and Testing.
Requirements:
- Fluent GERMAN is essential for this position and advanced English.
- 3 Years proven qualification/validation experience in the medical devices production environment.
- Experience in Process Validation, Medical Devices, 21 FDA 820, ISO 13485.
- Engineering background.
- Analytical, innovative and pragmatic thinking.
- Some flexibility in working hours is required.
- Able to follow change management for internal guidelines.
Are you interested in this position? Then we are looking forward to receiving your application.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik